CN111630028A

CN111630028A - Process for preparing methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate

Info

Publication number: CN111630028A
Application number: CN201980007447.2A
Authority: CN
Inventors: T.克瑙夫; P.普拉滕; D.曼策尔; S.韦斯霍芬
Original assignee: Covestro Intellectual Property GmbH and Co KG
Current assignee: Covestro Intellectual Property GmbH and Co KG
Priority date: 2018-01-05
Filing date: 2019-01-02
Publication date: 2020-09-04
Anticipated expiration: 2039-01-02
Also published as: US20200331848A1; EP3735405A1; WO2019134909A1; EP3735405B1; HUE057045T2; US10947187B2; PT3735405T; CN111630028B

Abstract

The invention relates to a method for producing methylene diphenylene diisocyanate and optionally mixtures of methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanates, wherein in step a) a fraction (142) comprising methylene diphenylene diisocyanate and minor components is provided, which is optionally carried out by step a.1): separating methylene diphenylene diisocyanate and minor components from a fraction (100) comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate, and wherein in step β) the fraction (142) comprising methylene diphenylene diisocyanate and minor components is subjected to a purification comprising isomer separation in two or more sub-steps (a, b, … …) by distillation and/or crystallization to obtain two or more pure methylene diphenylene diisocyanate fractions (140-1, 140-2, … …) and a minor component fraction (150), wherein the minor component fraction (150) obtained in step β) is recycled to one or more of the sub-steps of step β) in which no pure methylene diphenylene diisocyanate fraction (140-1) from step β) is obtained as distillate or crystal, 140-2, … …), and/or recycled to step α.1) if step α.1) is performed.

Description

Process for preparing methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate

The invention relates to a method for producing methylene diphenylene diisocyanate and optionally mixtures of methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanates, wherein in step a) a fraction comprising methylene diphenylene diisocyanate and minor components is provided, which is optionally carried out by step a.1): separating methylene diphenylene diisocyanate and minor components from the fraction comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate, and wherein in step β) the fraction comprising methylene diphenylene diisocyanate and minor components is subjected to a purification comprising an isomer separation by distillation and/or crystallization in two or more substeps, to obtain two or more pure methylene diphenylene diisocyanate fractions and a minor component fraction, wherein the minor component fraction obtained in step beta) is recycled to one or more of the sub-steps of step beta), in this substep no fraction of pure methylene diphenylene diisocyanate from step beta) is obtained as distillate or crystals, and/or, if step α.1) is carried out, recycled to step α.1).

Isocyanates (1) are prepared in large amounts and are used mainly as starting materials for the preparation of polyurethanes. They are usually prepared by reacting the corresponding amines (2) with phosgene (3), with a stoichiometric excess of phosgene being used. The reaction of the amines with phosgene can be carried out both in the gas phase and in the liquid phase, it being possible for the reaction to be carried out discontinuously or continuously (W. Siefken, LiebigsAnn. 562, 75-106 (1949)). The preparation of organic isocyanates from primary amines and phosgene has been described several times; by way of example only, reference is made to Ullmanns Encyklop ä die der technischen Chemie, 4 th edition (1977), Vol.13, p.351-: general 221(2001), 303-335, Elsevier Science B.V. Aromatic isocyanates such as methylene diphenylene diisocyanate (hereinafter MMDI- "monomeric MDI"), mixtures of MMDI and polymethylene polyphenylene polyisocyanates (which are higher homologues of MMDI, hereinafter PMDI, "polymeric MDI"; mixtures of MMDI and PMDI hereinafter collectively referred to as MDI) or Toluene Diisocyanate (TDI), and aliphatic isocyanates such as pentane 1, 5-diisocyanate (PDI), hexamethylene 1, 6-diisocyanate (HDI) or isophorone diisocyanate (IPDI) are of interest on an industrial scale. Furthermore, isocyanates having benzylic isocyanate groups are also important; particular mention should be made here of Xylylene Diisocyanate (XDI).

Modern industrial-scale production of isocyanates is carried out semicontinuously (some production steps being carried out discontinuously, for example discontinuous reaction and continuous work-up) or continuously (all steps being continuous).

The process scheme in the liquid phase, commonly referred to as liquid phase phosgenation, is characterized by: the reaction conditions are chosen such that at least the reaction components amine, crude isocyanate and phosgene, but preferably all reactants, products and reaction intermediates, are present as a liquid in a suitable solvent under the conditions chosen. After the conversion is complete, a gas phase comprising hydrogen chloride by-product and unconverted phosgene (since it is used in stoichiometric excess) is separated off; the desired isocyanate is substantially retained in the liquid phase together with the solvent. The crude isocyanate is thus obtained as a liquid stream in a mixture with a solvent, which is subsequently treated to obtain pure isocyanate (and the solvent and the dissolved phosgene and hydrogen chloride fractions are recovered).

Thus, in all industrial-scale relevant isocyanate preparation processes, a liquid crude isocyanate stream is obtained which has to be worked up to obtain the desired isocyanate in pure form and to recover other valuable substances, such as solvents. This work-up generally involves separating off the solvent, dissolved phosgene and dissolved hydrogen chloride. The isocyanate is then subjected to a fine purification, which may also include isomer separation, if desired. Depending on the type of isocyanate, homologue separation may be carried out before the fine purification. It should be mentioned in particular here that MMDI is partially separated from the isocyanate mixture which is substantially freed from solvent, phosgene and hydrogen chloride and contains MMDI and PMDI, in order to obtain MMDI fractions containing at most negligible traces of PMDI (crude MMDI) and mixtures of PMDI and MMDI.

The work-up of the crude isocyanate stream on an industrial scale is not trivial, since many different requirements have to be taken into account simultaneously. In addition to obtaining the target product in the form of as great a purity as possible, mention should be made here of recovering phosgene, hydrogen chloride and solvent with as little loss as possible, in particular in order to recycle them (optionally after further conversion, for example of hydrogen chloride into chlorine) into the process. All this has to be carried out under conditions which are as economically viable as possible, i.e. with as little energy consumption as possible and with as little loss of valuable products as possible (in particular isocyanates which, without optimally designed work-up, may enter into undesired further reactions).

The work-up by distillation of crude isocyanates, in particular crude MDI, and in particular crude MMDI, has been described many times.

DE3145010a1 relates to a process for preparing 4,4' -MMDI of high purity by: the 4,4'-MMDI isomer is distillatively separated from the MDI obtained from the phosgenation of aniline/formaldehyde condensates in a distillation stage (1), the top product obtained here is further distilled in a distillation stage (2), wherein from 0.5% to 20% by weight of the amount of product introduced into stage (2) is withdrawn as bottom product of stage (2), and subsequently 2,2' -and 2,4'-MMDI are separated from the fraction obtained as top product of stage (2) in a downstream distillation stage (3), and the bottom product obtained in stage (3) is worked up distillatively to obtain 4,4' -MMDI in high purity. The temperature at the outlet of the condenser of the distillation stages (1), (2) and (3) is adjusted to 130 ℃ to 230 ℃ in such a way that it is 10 ℃ to 100 ℃ lower than the vapor temperature predetermined in each case by the vacuum. Furthermore, the work-up of the bottom product obtained in stage (3) is carried out in two stages, so that in the first final stage (4) 50% to 90% by weight of the bottom product from stage (3) is separated as top product in the form of pure 4,4' -MMDI, and the bottom product from the first final stage (4) is divided in the second final stage (4') into a further portion of pure 4,4' -MMDI as top product and a distillation residue as bottom product.

EP1561746A2 describes a process for preparing a diisocyanate fraction of the diphenylmethane series, which fraction comprises at least 99% by weight, based on the mass of the fraction, of dicyclomethylene diphenyl diisocyanate, where

a) Aniline and formaldehyde are converted in the presence of an acidic catalyst into di-and polyamines of the diphenylmethane series comprising bicyclic methylenediphenyldiamine, and

b) phosgenating di-and polyamines of the diphenylmethane series comprising bicyclic methylenediphenyldiamine, optionally in the presence of a solvent, to obtain crude diisocyanates and polyisocyanates, and

c) separating a fraction containing at least 95% by weight of dicyclomethylene diphenyl diisocyanate, based on the mass of the fraction, from the crude diisocyanate and polyisocyanate, the fraction having a 4,4' -MDI content of 49% to 95.99% by weight, a2, 4' -MDI content of 4% to 45% by weight and a2, 2' -MDI content of 0.01% to 20% by weight, and

d) optionally removing 4,4' -MDI from the fraction obtained in step c) to an extent of 10% to 98%, and

e) removing 2,2'-MDI completely or partially from the fraction obtained in step c) or step d) to obtain a fraction comprising 0% to 0.4% by weight of 2,2' -MDI, 1% to 95% by weight of 4,4'-MDI and 5% to 98.6% by weight of 2,4' -MDI, based on the mass of the MDI isomers.

EP1686112A1 describes a process for preparing 2,4' -MMDI having a low 2,2' -MMDI content by distilling a mixture of isomeric diisocyanatodiphenylmethanes consisting of at least 2,2' -MMDI, 2,4' -MMDI and 4,4' -MMDI using at least one dividing wall column. A mixture containing 85 wt% to 99 wt% 2,4' -MMDI, up to 15 wt% 4,4' -MMDI and up to 0.2 wt% 2,2' -MMDI was obtained.

EP 1792895A 1 describes a process for preparing 4,4' -MMDI, in which

a) Aniline and formaldehyde in a molar ratio of 1.7-4:1 are converted in the presence of an acidic catalyst into di-and polyamines of the diphenylmethane series, and

b) reacting said diamines and polyamines with phosgene to the corresponding diisocyanates and polyisocyanates of the diphenylmethane series and optionally separating by distillation to obtain a mixture of diisocyanates and polyisocyanates of the diphenylmethane series (MDI) containing from 44% to 80% by weight of 4,4' -MMDI and a total of from 1% to 12% by weight of 2,4' -and/or 2,2' -MMDI and from 10% to 55% by weight of PMDI, based on the weight of the MDI, and

c) separating the MDI precisely into two fractions by distillation and/or crystallization, wherein a first fraction is obtained in an amount of 5-40 wt.% of the amount of MDI and a second fraction is obtained in an amount of 60-95 wt.% of the amount of MDI, and wherein the first fraction contains at least 97 wt.% 4,4' -MMDI and at most 3 wt.% 2,4' -MMDI based on the weight of the first fraction and the second fraction contains 30-60 wt.% 4,4' -MMDI, 1-12 wt.% 2,4' -MMDI and at most 2 wt.% 2,2' -MMDI and 35-65 wt.% PMDI based on the weight of the second fraction.

Although not always explicitly mentioned, all processes for preparing isocyanates result in secondary components which have a lower boiling point than the isocyanate to be prepared (so-called low boilers; for example phenyl isocyanate in the case of MDI preparation) and which have to be separated off as substantially as possible in the workup. The low boilers are generally sent to incineration via waste gas aftertreatment. The low boiler separation has the risk of entrainment of valuable products. The prior art does not, or at least does not adequately, address this problem.

As an alternative to or in particular in combination with the distillative workup, the crude isocyanate can also be worked up by crystallization, in particular melt crystallization and/or suspension crystallization. This is described, for example, in WO 2010/040675A 1 and WO 2013/081873A 1. If the isocyanate fraction is obtained by crystallization, the minor components (e.g.compounds having a boiling point lower than that of the desired isocyanate already mentioned) generally remain in the uncrystallized phase.

Therefore, regardless of the exact type of post-treatment, there is a need to further improve the post-treatment of crude MDI, in particular crude MMDI. In particular, it is desirable to separate the secondary components, in particular the so-called low boilers, from the desired target product with as little loss of valuable product as possible without impairing the economic viability of the process.

In view of this requirement, the subject of the present invention is a process for obtaining methylene diphenylene diisocyanate and optionally a mixture of methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate, comprising the steps of:

α) providing a fraction comprising methylene diphenylene diisocyanate and minor components, the mass proportion of which methylene diphenylene diisocyanate, based on its total mass and determined by gas chromatography, is greater than 98.0% (-) "Coarse MMDI"; stream 142 in the drawing), optionally via α.1)

α.1) separating methylene diphenylene diisocyanate and minor components from a fraction comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate ("crude MDI", stream 100 in the drawing) to obtain

(i) Polymethylene rich polymethylene polyisocyanates of methylene diphenylene diisocyanate and polymethylene polyphenylenepolyisocyanatesMixtures of phenylene polyisocyanates () "MDI", stream 141 in the drawing) and

(ii) a fraction (142) comprising methylene diphenylene diisocyanate and minor components, the mass proportion of methylene diphenylene diisocyanate being greater than 98.0% based on the total mass thereof and determined by gas chromatography;

beta) is purified by distillation and/or crystallization in two or more, preferably 3 to 10, more preferably 4 to 8, sub-steps (a, b, … …), including isomerizing the fraction (142) comprising methylenediphenylene diisocyanate and minor components to obtain at least

(i) Two or more, preferably 2 to 4, more preferably 2 to 3, pure methylene diphenylene diisocyanate fractions (140-1, 140-2, … …) each having a mass proportion of 99.9% or more, based on their total mass and determined by chromatography, and

(ii) a minor component fraction (150) having a mass proportion of methylene diphenylene diisocyanate, based on the total mass thereof and determined by chromatography, of from 20.0% to 98.0%,

wherein the minor component fraction (150) obtained in step β) is recycled to one or more of the sub-steps (a, b, … …) of step β) in which it is obtainedNone of the pure methylenedianiline from step β) was obtained as distillate or crystals Phenyl diisocyanate fraction (140-1, 140-2, … …)，

And/or, if step α.1) is carried out, recycled to step α.1).

The "providing" of the crude MMDI in step a) can be accomplished either by preparing the crude MMDI at the same production site where the purification of step β) was performed, or by preparing the crude MMDI elsewhere and transporting the crude MMDI to the production site where the purification of step β) was performed. In the latter case, the provision of step a) is simply achieved by taking the crude MMDI prepared elsewhere from a transport or storage tank or from a long distance pipeline.

A particularly suitable process, however, is an integrated process for the preparation and purification of MDI and MMDI,in which the step ofα) comprises Preparing at least a portion, and particularly all, of the crude MMDI to be purified in step β).Thus, in particular, a further subject of the present invention is a process for preparing methylene diphenylene diisocyanates (1a) and mixtures (1, MDI) of methylene diphenylene diisocyanates (1a) and polymethylene polyphenylene polyisocyanates (1b) from mixtures (2, MDA) of methylene diphenylene diamines (2a) and polymethylene polyphenylene polyamines (2b), which comprises the following steps:

A) -component of step α)-reacting MDA (2) with phosgene (3) in the presence of an organic solvent (4), wherein a stoichiometric excess of phosgene (3) based on all primary amino groups present is used, to obtain a liquid stream (60) comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate and secondary components (as well as organic solvent, dissolved hydrogen chloride and dissolved phosgene) and a gaseous stream (70) comprising hydrogen chloride and phosgene;

B) post-treating at least the liquid stream (60) comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate and minor components, which comprises:

B.I) -component of step α)-prepurification to isolate a first portion of the secondary components to obtain a liquid fraction (100) depleted of secondary components (as well as organic solvent, hydrogen chloride and phosgene) and comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate;

B.II)component of step α)Corresponding to step α.1) -separating methylene diphenylene diisocyanate and a further portion of the minor components from the fraction (100) depleted of minor components and comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate to obtain

(i) Polymethylene polyphenylene polyisocyanate-rich mixture of methylenediphenylene diisocyanate and polymethylene polyphenylene polyisocyanate (141 in the drawing, corresponding to 1) and

III) -corresponding to step beta) -purification by distillation and/or crystallization in two or more, preferably 3-10, more preferably 4-8 sub-steps (a, b, … …), including isomerizing the fraction (142) comprising methylenediphenylene diisocyanate and minor components to obtain at least

(i) Two or more, preferably 2 to 4, more preferably 2 to 3, pure methylene diphenylene diisocyanate fractions (140-1, 140-2, … … in the drawing; in each case corresponding to 1a), each having a proportion by mass of 99.9% or more, based on their total mass and determined by chromatography, of methylene diphenylene diisocyanate, and

wherein the fraction of minor constituents (150) obtained in step B.III)

Recycled to one or more of the sub-steps (a, b, … …) of step B.III), in which it is not necessary to add any additional additives to the mixtureNot as distillate The effluent or crystals are obtained as any pure methylene diphenylene diisocyanate fraction (140-1, 140- 2、……)，

And/or recycled to step B.II)

(see also fig. 1 in this case).

In this integrated process for the preparation and purification of MDI and MMDI, steps a), b.i) and b.ii) are an integral part of step α), wherein step b.ii) corresponds to step α.1). In addition, step b.iii) corresponds to step β).

According to the invention, "minor components" are understood to mean all constituents in the product stream and product fractions which do not correspond to the product of value to be produced (MMDI, MDI), nor are organic solvents, hydrogen chloride or phosgene. Examples of typical minor components in this sense are phenyl isocyanate (PHI) and acridine hydrochloride (which sublimes very easily and can therefore easily become an integral part of the distillate fraction). The minor component fraction (150) obtained in step β) or step b.iii) contains such minor components in a mass proportion of 2.0% to 80.0%, based on the total mass of the minor component fraction (150). In view of, for example, the toxicity of PHI (and in view of its monofunctional character), such a fraction cannot be used as a marketable valuable product even if the composition is at the lower end of said concentration range of the minor component; therefore, they are generally incinerated in the prior art.

In step β) or in step B.III)"substeps (a, b, … …)"This is understood here to mean a separation step in which the starting fraction, in particular the fraction (142) containing methylene diphenylene diisocyanate and minor components or the intermediate fraction obtained therefrom on the route leading to the final product, the pure methylene diphenylene diisocyanate fraction (140-1, 140-2, …), is separated into two or more, in particular two or three fractions. In the case of distillative purification, the separation step comprises in particular a distillation column familiar to the person skilled in the art (including the required peripheral equipment, such as evaporators, condensers, etc.). In the case of purification by crystallization, the separation step comprises in particular a crystallization reactor (also referred to as "crystallizer") familiar to the person skilled in the art.

"distillate" in the sense of the present invention means, according to the conventional terminology in the specialist literature, the fraction obtained by partial evaporation of the liquid distillation feed. The distillate in this sense is taken off at the top of the distillation column or as side draw. In contrast to the bottom stream from the distillation column (which is not regarded as distillate in the sense of the present invention), the distillate consists of the constituents of the liquid feed which have been transferred into the gas phase, optionally in addition to entrained traces of unvaporized feed liquid. The distillate is initially obtained in gaseous form and subsequently condensed. Such condensation can be carried out "specifically" on the one hand by sending the distillate initially obtained in gaseous form to the condenser. The "targeted condensation" in this sense can already take place in the distillation column itself (for example when a condenser is arranged in the region of or above the removal point of the distillate in the distillation column) or in a condenser arranged outside the distillation column after the distillate has been removed in gaseous form. On the other hand, depending on the exact configuration and operating mode of the distillation column, a liquid internal reflux can also be generated in the distillation column from the distillate obtained in gaseous form without contact with the condenser, which can be withdrawn in liquid form. Thus, depending on its design and its mode of operation, the distillate can be withdrawn from the distillation column in liquid or gaseous form.

"crystalline material" in the sense of the present invention means, according to the usual terminology in the specialist literature, a compound which crystallizes out of a mixture of liquid substances, i.e. precipitates out as a solid. The remaining liquid is referred to as mother liquor.

The following first presents a brief summary of various possible embodiments of the invention, a list of which should be considered non-exhaustive:

in a first embodiment of the invention, which can be combined with all other embodiments, step α.1) is included.

In a second embodiment of the present invention, which is a specific configuration of the first embodiment, the fraction (100) comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate is obtained by the steps of:

A) reacting a mixture (2) of methylenediphenylenediamine and polymethylene polyphenylene polyamine with phosgene (3) in the presence of an organic solvent (4), wherein a stoichiometric excess of phosgene (3) based on all primary amino groups present is used, to obtain a liquid stream (60) comprising methylenediphenylene diisocyanate and polymethylene polyphenylene polyisocyanate and secondary components and a gaseous stream (70) comprising hydrogen chloride and phosgene;

-prepurification to isolate a first portion of said secondary components to obtain a liquid fraction (100) depleted of said secondary components and comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate.

In a third embodiment of the present invention, which is a specific configuration of the second embodiment, the organic solvent (4) used in step a) is selected from monochlorobenzene, dichlorobenzene, dioxane, toluene, xylene, dichloromethane, perchloroethylene, trichlorofluoromethane and butyl acetate.

In a fourth embodiment of the present invention, which is a specific configuration of the second and third embodiments, the pre-purification comprises the steps of:

(1) separating a gas stream (90) comprising hydrogen chloride and phosgene from a stream (60) comprising methylene diphenylene diisocyanate, polymethylene polyphenylene polyisocyanate and minor components;

(2) separating a gas stream (110) comprising the organic solvent (4) from the liquid phase remaining after the separation of the gas stream (90) comprising hydrogen chloride and phosgene in step (1) to obtain a liquid fraction (100) depleted of secondary components and comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate;

and optionally

(3) The gas stream (110) comprising the organic solvent (4) is separated into a liquid stream (120) comprising the organic solvent (4) and a gas stream (130) comprising phosgene.

In a fifth embodiment of the invention as a particular configuration of the second to fourth embodiments, in step B) a gaseous stream (70) comprising hydrogen chloride and phosgene is also post-treated, wherein the post-treatment comprises:

separating phosgene from a gaseous stream (70) comprising hydrogen chloride and phosgene, in particular after combining with a gas stream (90) comprising hydrogen chloride and phosgene, to obtain a gas stream (170) comprising hydrogen chloride, wherein the gas stream (130) comprising phosgene, if present, is also subjected to the phosgene separation step;

and optionally a further step

Separating hydrogen chloride from the gas stream (170) comprising hydrogen chloride.

In a sixth embodiment of the present invention, which is a specific configuration of the second to fifth embodiments, step β) is performed by distillation.

In a seventh embodiment of the invention, which is a particular configuration of the sixth embodiment, step β) comprises 4 to 8 substeps, wherein each substep corresponds to a distillation in a distillation column without dividing walls, wherein the first pure methylene diphenylene diisocyanate fraction (140-1) and the second pure methylene diphenylene diisocyanate fraction (140-2) are each obtained as distillate in different distillation columns, wherein the minor component fraction (150) is obtained as distillate in a distillation column different from the distillation column used for obtaining the first and second pure methylene diphenylene diisocyanate fractions, wherein the third pure methylene diphenylene diisocyanate fraction (140-3) is obtained as bottom product in this distillation column.

In an eighth embodiment of the present invention, which is a specific configuration of the seventh embodiment, the minor component fraction (150) is fed to the feed of a distillation column in which the minor component fraction (150) has been obtained.

In a ninth embodiment of the invention, which is another specific configuration of the sixth embodiment, step β) comprises two or more substeps, at least one of which is carried out in a divided wall column.

In a tenth embodiment of the invention, which is a particular configuration of the ninth embodiment, in step β), the stream (142) comprising methylene diphenylene diisocyanate and minor components obtained in step α.1) is introduced into a dividing wall column, from which two prepurified methylene diphenylene diisocyanate fractions (140-11, 140-22) are withdrawn as sidestreams in liquid form and from which an overhead stream comprising minor components and methylene diphenylene diisocyanate is withdrawn,

wherein the prepurified methylene diphenylene diisocyanate fraction (140-11, 140-22, … …) is subjected to a fine purification in a further distillation stage to produce a first and a second pure methylene diphenylene diisocyanate fraction (140-1, 140-2),

wherein an overhead stream comprising the minor components and methylene diphenylene diisocyanate from a dividing wall column is distilled in a distillation column, which may optionally be designed as a side draw column with or without dividing walls, to obtain a minor component fraction (150) as an overhead stream, a third pure methylene diphenylene diisocyanate fraction (140-3) as a bottom stream and optionally a fourth pure methylene diphenylene diisocyanate fraction (140-4) as a side stream,

wherein the minor component fraction (150) is recycled to step α.1) or to the dividing wall column from step β).

In an eleventh embodiment of the invention, which can be combined with all embodiments in which step β) is not carried out purely by distillation, step β) comprises at least one substep in which crystallization is carried out, wherein the crystals obtained in the crystallization are a pure methylene diphenylene diisocyanate fraction or can be converted into a pure methylene diphenylene diisocyanate fraction by further purification.

In a twelfth embodiment of the invention, which is a particular configuration of the eleventh embodiment, the mother liquor obtained in the at least one sub-step in which the crystallization is carried out is distilled in at least two further sub-steps, wherein at least one further pure methylene diphenylene diisocyanate fraction and a minor component fraction (150) are obtained.

In a thirteenth embodiment of the invention as a specific configuration of the twelfth embodiment, the mother liquor is distilled in three further sub-steps, wherein two pure methylene diphenylene diisocyanate fractions are obtained.

The above briefly summarized embodiments of the present invention and other possible configurations are set forth in more detail below. The various embodiments may be arbitrarily combined with each other, except where the contrary is apparent to those of skill in the art from the context. The detailed description is made here on the basis of an integrated process for the preparation and purification of MDI, but this should not be understood as limiting.

Figure 1 shows, purely schematically, in its broadest form, an integrated process for the preparation and purification of MDI according to the present invention. The separation of organic solvent, hydrogen chloride, phosgene and the first part of the secondary components in step B.I) is schematically indicated by the upward arrow. According to the invention, a minor constituent fraction (150)Recycling to one of the sub-steps (a, b, … …) of step B.III) One or more, in which no pure methylene diphenylene diisocyanate stage from step B.III) is obtained Is divided (140-1, 140-2, … …), and/or recycled into step B.II)Is indicated by a "dashed line" arrow. The representation as the latter variant in the feed stream (100) is not to be understood as limiting; of course, the recycling can also be carried out by feeding the minor component fraction (150) to step (b.ii) separately from stream (100).

The continuous or semi-continuous, preferably continuous, production of MDI from MDA in step A) can be carried out by one of the methods known from the prior art. Suitable processes are described, for example, in EP 2077150 a1, EP 1616857 a1, EP 1873142 a1, EP 0716079 a1 and EP 0314985B 1. The concentrations and flow rates of the reactants amine (2) and phosgene (3) are preferably selected here such that a molar ratio of phosgene to primary amino groups of from 1.1: 1 to 30: 1, more preferably from 1.25: 1 to 3: 1, is established in the mixing of the co-reactants.

According to the invention, an organic solvent (4) is used in step A). Suitable organic solvents (4) which can be used according to the invention are in this case solvents which are inert under the reaction conditions, for example monochlorobenzene, dichlorobenzene (in particular the ortho-isomer), dioxane, toluene, xylene, dichloromethane, perchloroethylene, trichlorofluoromethane or butyl acetate. The inert solvent (4) is preferably substantially free of isocyanate (target mass proportion < 100 ppm) and substantially free of phosgene (target mass proportion < 100 ppm), which should be taken into account when using recycle streams. Therefore, it preferably works by the method described in EP 1854783 a 2. The solvents mentioned may be used alone or in the form of any mixture of the solvents mentioned by way of example. Preference is given to using Monochlorobenzene (MCB) or ortho-dichlorobenzene (ODB). MCB is very particularly preferred.

In step B), at least the liquid stream (60) comprising methylenediphenylene diisocyanate and polymethylene polyphenylene polyisocyanate and secondary components is worked up.

The prepurification of the liquid stream (60) comprising methylenediphenylene diisocyanate and polymethylene polyphenylene polyisocyanate and minor components (and also organic solvent, dissolved hydrogen chloride and dissolved phosgene) in step b.i) here preferably comprises the following steps:

(1) separating a gas stream (90) comprising hydrogen chloride and phosgene from a stream (60) comprising methylene diphenylene diisocyanate, polymethylene polyphenylene polyisocyanate and minor components (as well as organic solvent, dissolved hydrogen chloride and dissolved phosgene);

and optionally

In this embodiment, the liquid stream (100) depleted in minor components and comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate is thus the liquid phase left after separation of the gas stream (110) comprising organic solvent (4).

In step b.ii) the methylene diphenylene diisocyanate and a further portion of the secondary components are separated from the fraction (100) depleted of secondary components and comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate by distillation, crystallization or a combination of both, preferably by distillation.

In step b.iii), the fraction (142) comprising methylenediphenylene diisocyanate and minor components is purified in two or more sub-steps (a, b, … …), again by distillation, crystallization or a combination of both, preferably by distillation, including isomer separation.

Preferably, in step B), the gaseous stream (70) comprising hydrogen chloride and phosgene is also subjected to a work-up, wherein the work-up then comprises the following steps:

iv) separating phosgene from a gaseous stream (70) comprising hydrogen chloride and phosgene, in particular after combining with a gas stream (90) comprising hydrogen chloride and phosgene, to obtain a gas stream (170) comprising hydrogen chloride, wherein the gas stream (130) comprising phosgene, if present, is also subjected to the phosgene separation step;

and optionally

B.V) separating hydrogen chloride from the gas stream (170) comprising hydrogen chloride.

One possible configuration of the integrated process of the invention comprising steps a), b.i) (1), (2), (3), b.iv) and b.v) is set forth below with reference to fig. 2 (for the sake of simplicity of the drawing, the recycling of the minor component fraction (150) important for the invention has not been shown here; reference is made to the detailed figures 3a-b) discussed later herein.

In step A), MDA (2) and phosgene (3) are conveyed from the respective storage vessels (1020, 1030) to a suitable mixing zone (1100) and mixed there. This is carried out in the form of a solution (20, 30) in a solvent (4). Suitable means for configuration of the mixing zone (1100) are well known from the prior art. Mention may be made, by way of example, of static mixing units (preferably nozzles) and dynamic mixing units (preferably rotor-stator mixers). After mixing, the reaction mixture (50) is introduced into the reaction zone (1200). This is a residence time device in which the mixture obtained in the mixing zone (1100) gets enough opportunity to react to completion. Suitable apparatuses are well known from the prior art (for example, vertically arranged tubular reactors flowing from bottom to top, so-called "phosgenation columns"). The separation of the crude process product into a liquid phase (60) and a gaseous stream (70) comprising hydrogen chloride and phosgene is carried out in the actual reaction zone itself or in a separation zone (1210). It is also possible to integrate the mixing zone and the reaction zone or the mixing zone, the reaction zone and the separation zone or the reaction zone and the separation zone into a single apparatus (for example into the respective reactor). According to the invention, it is also possible to connect a plurality of mixing zones and/or reaction zones and/or, if present, separator zones in series or in parallel; for example in the form of a cascade of a plurality of reactors in series. The process product obtained in the reaction zone (1200) is separated into a liquid phase (60) which, in addition to MDI, contains dissolved hydrogen chloride, excess dissolved phosgene, solvent and secondary components, and a gaseous stream (70) which contains hydrogen chloride gas, phosgene and gaseous solvent. The reaction zone may be followed, if desired, by a device for cleaving carbamoyl chlorides (not shown in FIG. 2). In such a case, the liquid phase (60) passes through the apparatus, which then undergoes a work-up in step B). The hydrogen chloride-rich gas phase produced here is preferably combined with the gaseous stream (70) and worked up further together.

The post-treatment of the crude isocyanate in step B) comprises: firstly in step b.1), by passing the mixture through a distillation apparatus (2100; so-called "phosgene removal column") into a liquid stream (80) comprising solvent and isocyanate and a gaseous gas stream (90) comprising phosgene and hydrogen chloride, the phosgene and hydrogen chloride being depleted from the liquid phase (60) of step a). The so-called "stripper" can be operated by any method known in the art, preferably as described in EP 1854783B 1, especially in paragraphs [0018] and [0023 ].

The liquid stream (80) thus obtained is separated in a distillation apparatus (2200; so-called "solvent column") into a gas stream (110) still containing solvent and an isocyanate-containing liquid stream (100). This can be carried out by any method known in the art, preferably as described in EP 1854783B 1, especially paragraphs [0024] to [0027 ]. The distillation apparatus (2200) may also comprise two or more columns (this possibility is not shown in fig. 2 for the sake of simplicity of the drawing).

The process waste gas stream (110), preferably after liquefaction in a condenser (2310), is separated in a distillation apparatus (2300; so-called "solvent stripper") into a liquid stream (120) containing solvent and a gas stream (130) containing phosgene. This can be performed by any method known in the art, preferably as described in EP 1854783B 1, especially paragraphs [0027] and [0028 ].

The phosgene-containing gas streams (70), (90) and (130) thus obtained are cleaned (i.e. freed of a major amount of phosgene) by absorption in a solvent (4) in an absorption apparatus (2500; so-called "phosgene absorber") to obtain a liquid stream (160) comprising solvent and phosgene and a gaseous process off-gas stream (170) comprising hydrogen chloride and solvent, wherein preferably the phosgene-containing gaseous process off-gas streams (70) and (90) are first combined and the combined phosgene-containing process off-gas stream from (70) and (90) and the phosgene-containing process off-gas stream (130) are each condensed and then introduced into the absorption apparatus (2500) in liquid form (step b.iv)). The cleaning may be performed by any method known in the art, preferably as described in EP 2093215 a 1.

The phosgene-containing gas stream (170) obtained in this way contains hydrogen chloride formed in the reaction and is therefore preferably passed to a separation unit (2600) for separating off hydrogen chloride (step b.v)). The hydrogen chloride component is preferably depleted by absorption of hydrogen chloride in water or dilute hydrochloric acid as absorbent (180) in a further absorption apparatus (2600; "HCl absorption column") to obtain a stream (190) comprising hydrochloric acid, and preferably after passage through a vapor condenser (2630) to substantially separate liquefiable components (191), a gaseous phosgene-containing process off-gas stream (200) comprising solvent and optionally gaseous secondary components is obtained. This step may be performed by any method known in the art. This mode of operation is preferably as described in EP 1743882B 1, especially paragraphs [0027] to [0028 ].

The absorbent (180) used is water (e.g. steam condensate) or hydrochloric acid (dilute hydrochloric acid) in a concentration of 0.50% to 15.0% by mass. The solvent contained in the stream (170) is transferred mainly to the gas stream (200) by the heat released in the absorption of hydrogen chloride.

The phosgene-containing process exhaust gas stream (200) obtained in this way is passed to phosgene decomposition (apparatus 3000, C); it preferably comprises two (or more) phosgene decomposition units (3011 and 3012) connected in parallel, operated alternately and regenerated. The aqueous stream is used here to decompose phosgene in a catalytic manner, preferably on activated carbon, to obtain a gaseous stream comprising the optional solvent and the optional gaseous secondary components and a liquid stream comprising hydrochloric acid. Preferably, the process off-gas and the aqueous stream are co-currently directed through the activated carbon bed. The gaseous process off-gas stream (210) leaving the phosgene decomposition unit is then sent to an incineration unit (unit 6000, D)), optionally after passing through an adsorption unit (not shown in fig. 2) for separating out the last solvent residues.

To purify crude MDI (crude MDI 100) which has been substantially freed from solvents, phosgene and hydrogen chloride, the MMDI is first partly separated off in a so-called "polymer separation" (apparatus 2410) (step B.II). The polymer separation can be carried out by distillation, crystallization or a combination of both, preferably by distillation. In each case, a fraction (142) is obtained which, in addition to the MMDI, also contains a further part of the secondary components contained in the initially obtained liquid crude product (60) (monomer fraction, so-called crude MMDI). Step b.ii) is configured in particular such that minor components of low boiling point or volatility relative to MMDI (for example PHI or solvent residues which have not been completely separated off in the preceding step) are separated off as far as possible together with the monomer fraction, so that the remaining mixture of methylenediphenylene diisocyanate and polymethylene polyphenylene polyisocyanate (the so-called polymer fraction, 141) already has the purity required for further use. This is best achieved by distillative separation. Thus, the crude MDI (stream 100) is preferably separated in a distillation column (2410) into a distillate fraction comprising MMDI and minor components (stream 142) and a PMDI-rich mixture of MMDI and PMDI (stream 141, bottom stream). Possible configurations for this purpose are known to the person skilled in the art and are described, for example, in EP1561746A2, in particular paragraph [0038] and in the examples, and in DE3145010A1, in particular page 7, line 17 and beyond, and in FIG. 1.

According to the invention, the crude MMDI (142) thus separated contains more than 98.00 mass% MMDI based on its total mass. The remaining MDI mixture (141) of MMDI and PMDI is widely used in polyurethane chemistry as such or after addition of the MMDI-containing stream obtained in step b.iii).

The monomer fraction (142) obtained in step b.ii) can be fed-directly or after temporary storage in a tank vessel-to step b.iii), into which tank vessel optionally also an otherwise provided monomer fraction comprising, based on its total mass and as determined by gas chromatography, greater than 98.0% by mass of methylenediphenylene diisocyanate and secondary components is fed.

The monomer fraction (120) is purified in step B.III) in two or more substeps (a, b, … …), in particular at least obtained

(i) Two or more pure methylene diphenylene diisocyanate fractions (140-1, 140-2, … …) each having a mass proportion of 99.9% or more, based on the total mass thereof and determined by chromatography, and

(ii) the minor component fraction (150) has a mass proportion of methylene diphenylene diisocyanate, based on its total mass and determined by chromatography, of 20.0% to 98.0%.

The purification in step b.iii) can be carried out by distillation, crystallization or a combination of both, preferably by distillation. To simplify the drawing, this step is shown purely schematically in overview fig. 2. Reference numeral 2400 and the assigned symbols generally represent a plurality of post-processing units herein. A possible configuration for the preferred distillative purification is shown below with reference to more detailed figures 3 a-b.

Fig. 3a shows a possible configuration of step b.iii) of the process according to the invention, using six distillation columns (2400-1 to 2400-6) without dividing walls. To simplify the drawing, peripheral devices such as pumps, condensers and tanks are omitted. Each of the distillates (first obtained in gaseous form) was brought to a temperature of 50 ℃ to 150 ℃ and 5 mbar_(Absolute)-15 mbar_(Absolute)Is condensed under pressure of (a). The temperature chosen depends on the composition of the isomer mixture of the respective distillate. Those components of the respective distillate which do not condense under the respective pressure and temperature conditions are discharged into a vacuum system and finally into an exhaust system. Finally, the low boilers (components having a boiling point below 2,2' -MMDI) are also removed from the distillation system in this way; but with significantly less isocyanate loss compared to the prior art.

In a first substep (a), the stream (142) comprising MMDI and minor components from step b.ii) is introduced into a distillation column (2400-1). In the distillation column, the relatively high-boiling secondary components and optionally entrained PMDI constituents are separated off as a bottom stream (143). The bottom stream furthermore comprises a proportion of monomers, in particular a proportion of the highest-boiling isomer 4,4' -MMDI. The stream (143) has a proportion by mass of methylene diphenylene diisocyanate of less than 99.9% (i.e. in particular from 50.0% to 99.5%) based on its total mass and determined by gas chromatography and can be blended, for example, with the MDI fraction (141) obtained in step b.ii.

The distillate obtained in the first distillation column is now transferred in the second substep (b) into another distillation column (2400-2). The bottoms from this column contain predominantly the highest boiling isomer, 4'-MMDI, with a small proportion of 2,4' -MMDI, while the distillate (overhead) is a mixture of all isomers. In order to increase the operational reliability, it may be expedient to provide two parallel-connected, alternately operable distillation columns (not shown in fig. 3 a) for substep (b).

Now in the third substep (c), the distillate from the distillation column (2400-2) is introduced into a further distillation column (2400-3), in which the low-boiling secondary components are separated off together with the MMDI isomer components as distillate.

In a fourth substep (d), the bottom product from the third distillation column (2400-3) is transferred to another distillation column (2400-4), in which a first pure MMDI fraction (140-1) comprising mainly the isomers 4,4' -MMDI and 2,4' -MMDI and a minor proportion of 2,2' -MMDI is obtained as distillate. The pure MMDI fraction (140-1) preferably contains 0.0 mass% to 2.0 mass% 2,2'-MMDI, 30.0 mass% to 70.0 mass% 2,4-MMDI and 30.0 mass% to 70.0 mass% 4,4' -MMDI, based on the total mass of all MMDI isomers.

In the fifth substep (e), the bottom product from the second distillation column (2400-2) was introduced into the distillation column (2400-5). There a second pure MMDI fraction (140-2) containing mainly 4,4' -MMDI isomer is obtained as distillate. It is also conceivable to use, instead of a single distillation column (2400-5), two distillation columns (2400-51, 2400-52) connected in series, wherein a second pure MMDI fraction (140-2) (not shown in fig. 3 a) is then obtained as distillate from the second distillation column (2400-52) in the flow direction. In this embodiment, the separation of substances carried out in each of the distillation columns 2400 to 51 and 2400 to 52 is to be regarded as a separate sub-step in the sense of the present invention. In each case, the pure MMDI fraction (140-2) preferably contains 0.0 mass% to 1.0 mass% 2,2'-MMDI, 0.1 mass% to 5.0 mass% 2,4-MMDI and 94.0 mass% to 99.9 mass% 4,4' -MMDI, based on the total mass of all MMDI isomers.

The bottom product from the fifth distillation column (2400-5) was fed to the fourth distillation column (2400-4) together with the bottom product from the third distillation column (2400-3).

In the sixth substep (f), the distillate from the third distillation column (2400-3) was transferred to another distillation column (2400-6, so-called "low boiler column"). There, the minor component fraction (150) was separated as distillate, while a third pure MMDI fraction (140-3) containing all isomers was obtained as bottom product. It can be used further as such or blended with other fractions, for example with the MDI fraction (140) obtained in step b.ii). The pure MMDI fraction (140-3) preferably contains 10.0 mass% to 60.0 mass% 2,2'-MMDI, 30.0 mass% to 80.0 mass% 2,4-MMDI and 0.0 mass% to 20.0 mass% 4,4' -MMDI, based on the total mass of all MMDI isomers. The minor component fraction (150) preferably has a proportion by mass of methylene diphenylene diisocyanate of from 20.0% to 98.0%, preferably from 60% to 98%, based on its total mass.

It is now important for the invention that the minor component fraction (150) is recycled to the point of work-up where no pure methylene diphenylene diisocyanate fraction (140-1, 140-2, … …) from step B.III) is obtained as distillate. In this regard, fig. 3a shows possible implementation variants for this embodiment (indicated by the "dashed" arrows): the minor component fraction (150) may-after being substantially liquefied; see above-transfer to the feed of the first distillation column (2400-1) and/or to the feed of the second distillation column (2400-2) and/or to the feed of the third distillation column (2400-3) and/or to the feed of the sixth distillation column (2400-6). For energy reasons, preference is given to feeding only to the feed of the sixth distillation column (2400-6).

It was found, entirely surprisingly, that this mode of operation does not lead to an unacceptable enrichment of the low boilers in the valuable product stream, but rather the low boilers are discharged (and ultimately incinerated) to a sufficient extent by means of an offgas system. The process of the present invention thus allows partial to complete utilization of the MMDI components contained in the minor component fraction (150), which may in any case constitute up to 98.0 mass-% of the stream, without adversely affecting the product quality.

Unlike the embodiment of fig. 3a, it is also possible to carry out step b.iii) using a dividing wall column and thus to reduce the number of distillation columns required. This is shown in fig. 3b in an embodiment where only four distillation columns (2400-1 to 2400-4) are sufficient. To simplify the drawing, peripheral devices such as pumps, condensers and tanks are omitted. The respective distillate, which is initially obtained in gaseous form, is brought in a respective distillation column or in an externally located condenser to a temperature of 50 ℃ to 150 ℃ and 5 mbar_(Absolute)-15 mbar_(Absolute)Is condensed under pressure of (a). The temperature chosen depends on the composition of the isomer mixture of the respective distillate. Those components of the respective distillate which do not condense under the respective pressure and temperature conditions are discharged into a vacuum system and finally into an exhaust system.

In a first substep (a), the stream (142) comprising MMDI and minor components from step b.ii) is introduced into a distillation column (2400-1) with dividing wall, the so-called dividing wall column. Two side streams are withdrawn from the dividing wall column in liquid form:

the upper side stream (140-11) contains a mixture of all isomers and is subjected in a second substep (b) to a fine purification in a second distillation column (2400-2) without dividing walls, in order to obtain a pure MMDI fraction (140-1) as distillate. The pure MMDI fraction (140-1) preferably contains 0.0 mass% to 2.0 mass% 2,2'-MMDI, 30.0 mass% to 70.0 mass% 2,4-MMDI and 30.0 mass% to 70.0 mass% 4,4' -MMDI, based on the total mass of all MMDI isomers.

The lower side stream (140-22) contains predominantly the highest boiling isomer 4,4'-MMDI and a small proportion of 2,4' -MMDI and is subjected in a third substep (c) to a fine purification in a third distillation column (2400-3) without dividing walls to obtain a pure MMDI fraction (140-2) as distillate. The pure MMDI fraction (140-2) preferably contains 0.0 mass% to 1.0 mass% 2,2'-MMDI, 0.1 mass% to 5.0 mass% 2,4-MMDI and 94.0 mass% to 99.9 mass% 4,4' -MMDI, based on the total mass of all MMDI isomers.

Transferring the bottom stream obtained in substeps (b) and (c) to the feed of the dividing wall column.

The bottom stream (143) obtained in the dividing wall column contains relatively high-boiling minor components and optionally entrained PMDI constituents. The bottom stream additionally comprises monomeric constituents, in particular constituents of the highest-boiling isomer 4,4' -MMDI. The stream (143) has a proportion by mass of methylene diphenylene diisocyanate of less than 99.9% (i.e. in particular from 50.0% to 99.5%), based on its total mass and determined by gas chromatography, and can be blended, for example, with the MDI fraction (141) obtained in step b.ii).

The top stream obtained in the dividing wall column contains low-boiling minor components as well as MMDI constituents. In a fourth substep (d), this stream is purified in a distillation column (2400-4) configured as a side draw column (without dividing wall in fig. 3 b; a dividing wall column can also be used at this location) to remove minor components which are withdrawn overhead as a minor component fraction (150), while a third pure MMDI fraction (140-3) containing all isomers is obtained as bottom product. It can be used further as such or blended with other fractions, for example with the MDI fraction (140) obtained in step b.ii). The pure MMDI fraction (140-3) preferably contains 10.0 mass% to 60.0 mass% 2,2'-MMDI, 30.0 mass% to 80.0 mass% 2,4-MMDI and 0.0 mass% to 20.0 mass% 4,4' -MMDI, based on the total mass of all MMDI isomers. The side draw stream (140-4) typically has an isomer distribution also within this range, but typically contains more minor components. However, the requirements for a pure MMDI fraction (up to 0.1% minor components) were met. In principle, it is also conceivable to operate the distillation column (2400-4) without side draw; depending on the mode of operation, the MMDI components and minor components contained in the side draw stream in this case in the embodiment according to fig. 3b pass into the minor component fraction (150) withdrawn overhead or into the bottom stream (140-3).

In this embodiment, the minor component fraction (150) -after being substantially liquefied; see above-transfer to the feed of dividing wall column (2400-1).

In all embodiments outlined above, the minor component fraction (150) may also be recycled to step b.ii) (polymer isolation). To this end, the minor component fraction (150) -after substantial liquefaction; see above-may be transferred to the feed to distillation column (2410).

The bottom stream (140-3) obtained in the above embodiments, after mixing with other pure MMDI fractions, can be used in many fields, if desired. In particular, mention should be made at this location of use in the manufacture of sports floors, flexible foams and food packaging and use as wood adhesives.

In addition to the above-described embodiment with a pure distillation configuration of step b.iii), it may also comprise a crystallization step. Examples of such embodiments can be found, for example, in EP1561746a2 and in document WO2010/095927a1 cited therein, as well as m. Stepanski and p. Faessler, SULZER Technical REVIEW 4/2002, pages 14 to 16.

A combination of crystallization and distillation steps is preferred. For example, in the embodiment according to fig. 3a, the separation task of the second distillation column (2400-2) can be replaced by a crystallization step in which the highest boiling 4,4'-MMDI isomer as well as a small proportion of 2,4' -MMDI is crystallized out, while a mixture of all isomers remains as mother liquor. The mother liquor can then be worked up by distillation in at least two further substeps to obtain at least one pure methylene diphenylene diisocyanate fraction. This is preferably done in three substeps in the distillation columns 2400-3, 2400-4 and 2400-6 in the manner described above to obtain two pure methylene diphenylene diisocyanate fractions (140-1 and 140-3). For further purification to obtain a pure MMDI fraction (140-2), the crystallisate with a high 4,4' -MMDI content can be subjected to a second crystallization, or-after liquefaction-distilled in a distillation column 2400-5. However, this further purification is not absolutely necessary; if the crystallization instead of the distillation in distillation column 2400-2 already provided a pure MMDI fraction (140-2) of sufficient purity, no further crystallization or distillation in distillation column 2400-5 need be performed.

Also important to the invention in embodiments comprising a crystallization step, is the location where the minor component fraction (150) is recycled to the work-up without obtaining any pure methylene diphenylene diisocyanate fraction (140-1, 140-2, … …) from step b.iii) as distillate or crystals. This means that the minor component fraction (150) is not recycled to sub-step (b) when sub-step (b) is replaced by crystallization which already provides the desired pure MMDI fraction (140-2) in sufficient purity to avoid the need for further distillation or crystallization steps.

Example (b):

the analysis method comprises the following steps:

viscosity: measured by a falling ball viscometer or a Brookfield viscometer (rotational viscometer).

NCO value: reacted with dibutylamine and back titrated with standard HCl solution for unconverted dibutylamine.

Consists of the following components: gas chromatography.

In examples 1-4, steps a) and b.i) (where the amount of MDA converted may be different) are performed as described in WO2017/050776 a1, page 35, line 2 to page 36, line 10). In example 5, the corresponding conditions were used as the basis for the process simulation.

In examples 1 to 3, the crude MDI obtained in this way as the bottom product was subjected to "polymer separation" according to step b.ii) as follows (see also fig. 2):

the crude MDI (corresponding to stream 100 in FIG. 2, flow rate 5.4t/h) was separated in a distillation column (2410) into a fraction containing MMDI and minor components (separation of minor components such as phenyl isocyanate and solvent in the previous step was not 100% successful) (crude MMDI; stream 142, 1.8t/h) and a PMDI-rich mixture of MMDI and PMDI (MDI; stream 141, 3.6 t/h). The distillation column (2410) is operated at 8 mbar_(Absolute)The operation was carried out under pressure and at a bottom temperature of 220 ℃.

In example 4, step b.ii) was carried out in a side draw column (without dividing wall; feed 63t/h) at 10 mbar_(Absolute)Pressure and a bottom temperature of 225 ℃, whereby crude MMDI (142) is withdrawn as a side stream. In example 5, the correspondingAs a basis for process simulation.

The fractions (142) containing MMDI and minor components obtained in each of examples 1-4 in this way were pumped into a storage tank (not shown in fig. 2). The fraction (142) was removed from the tank as starting material for the following examples.

Example 1 (comparative example-distillation column without dividing wall)

The recycling of the minor component fraction (150) is excluded, purification and isomer separation are carried out by the process according to fig. 3a (minor component fraction (150) is incinerated). The following operating parameters are followed here:

table 1:operating parameters in example 1

The following streams leave the distillation sequence:

table 2:product stream obtained in example 1

Example 2 (invention-distillation column without dividing wall)

The process is as in example 1 except that the minor component fraction (150) is used as an integral part of the feed to distillation column 2400-1. The following operating parameters are followed here:

table 3:operating parameters in example 2

The following streams leave the distillation sequence:

table 4:product stream obtained in example 2

Example 3 (Hair StichesMing-distillation column without dividing wall)

The process is as in example 1 except that the minor component fraction (150) is used as an integral part of the feed to distillation columns 2400-6. For this purpose, stream 150 is mixed with the distillate from distillation column 2400-3. The following operating parameters are followed here:

table 5:operating parameters in example 3

The following streams leave the distillation sequence:

table 6:product stream obtained in example 3

Examples 1-3 show that the recycling of the minor component fraction (150) of the present invention enables the yield of the high purity fraction 140-3 to be increased (since less isocyanate is transferred to incineration with the minor component fraction (150)), especially without a significant increase in the minor component content of any valuable stream product.

Example 4 (comparative example; distillation column with dividing wall)

Purification and isomer separation was performed by the method according to fig. 3b, with the following exceptions:

the minor component fraction (150) is not recycled to the feed of the dividing wall column but is incinerated.

The following operating parameters are followed here:

table 7:operating parameters in example 4

The following streams leave the distillation sequence:

table 8:product stream obtained in example 4

Table 8 (next):product stream obtained in example 4

Example 5 (inventive-distillation column without dividing wall; method simulation)

The process is as shown in figure 3b (i.e. in contrast to example 4, the minor component fraction (150) is not incinerated, but recycled to the feed to the dividing wall column), but otherwise is carried out under the same operating conditions as in example 4. The yield of stream 140-3 is increased by 0.10t/h and reaches 0.90t/h, wherein the composition in stream 140-3 remains essentially the same (less isocyanate is introduced to the incineration via the minor component fraction (150), without the product quality being impaired).

Claims

1. A process for preparing methylene diphenylene diisocyanate and optionally a mixture of methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate, the process comprising the steps of:

a) providing a fraction (142) comprising methylene diphenylene diisocyanate and minor components, the mass proportion of which methylene diphenylene diisocyanate, based on its total mass and determined by gas chromatography, is greater than 98.0%, which is optionally carried out by a.1)

α.1) separating methylene diphenylene diisocyanate and minor components from a fraction (100) comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate to obtain

(i) Polymethylene polyphenylene polyisocyanate-rich mixture of methylenediphenylene diisocyanate and polymethylene polyphenylene polyisocyanate (141) and

the method is characterized in that: subjecting the minor fraction (150) obtained in step β)

Recycled to one or more of the substeps (a, b, … …) of step β), in which no fraction of pure methylene diphenylene diisocyanate (140-1, 140-2, … …) from step β) is obtained as distillate or crystals,

and/or, if step α.1) is carried out, recycled to step α.1).

2. The method of claim 1, comprising step α.1).

3. The process according to claim 2, wherein the fraction (100) comprising methylene diphenylene diisocyanate and polymethylene polyphenylene polyisocyanate is obtained by:

4. The process according to claim 3, wherein the organic solvent (4) used in step A) is selected from the group consisting of monochlorobenzene, dichlorobenzene, dioxane, toluene, xylene, dichloromethane, perchloroethylene, trichlorofluoromethane and butyl acetate.

5. The method of claim 3 or 4, wherein the pre-purification comprises:

and optionally

6. The process as claimed in any of claims 3 to 5, wherein in step B) the gaseous stream (70) comprising hydrogen chloride and phosgene is also subjected to a work-up, wherein the work-up comprises:

and optionally a further step

7. The process according to any one of claims 3 to 6, wherein step β) is carried out by distillation.

8. The process as claimed in claim 7, wherein step β) comprises 4 to 8 substeps, wherein each substep corresponds to a distillation in a distillation column without dividing walls, wherein the first pure methylene diphenylene diisocyanate fraction (140-1) and the second pure methylene diphenylene diisocyanate fraction (140-2) are each obtained as distillate in different distillation columns, wherein the minor component fraction (150) is obtained as distillate in a distillation column different from the distillation column used for obtaining the first and second pure methylene diphenylene diisocyanate fractions, wherein the third pure methylene diphenylene diisocyanate fraction (140-3) is obtained as bottom product in this distillation column.

9. The process as claimed in claim 8, wherein the minor component fraction (150) is fed to a feed of a distillation column in which the minor component fraction (150) has been obtained.

10. The process of claim 7, wherein step β) comprises two or more substeps, wherein at least one substep is carried out in a divided wall column.

11. The process as claimed in claim 10, wherein in step β), the stream (142) obtained in step α.1) comprising methylene diphenylene diisocyanate and minor components is introduced into a dividing wall column, two prepurified methylene diphenylene diisocyanate fractions (140-11, 140-22) are taken off from the dividing wall column in liquid form as side streams, and an overhead stream comprising minor components and methylene diphenylene diisocyanate is taken off from the dividing wall column,

12. A process as claimed in any of claims 1 to 6, wherein step β) comprises at least one substep in which crystallization is carried out, wherein the crystals obtained in the crystallization are a fraction of pure methylene diphenylene diisocyanate or can be converted into a fraction of pure methylene diphenylene diisocyanate by further purification.

13. The process as claimed in claim 12, wherein the mother liquor obtained in the at least one sub-step in which the crystallization is carried out is distilled in at least two further sub-steps, wherein at least one further fraction of pure methylene diphenylene diisocyanate and a fraction of minor components (150) are obtained.

14. The process of claim 13, wherein the mother liquor is distilled in three further substeps, wherein two pure methylene diphenylene diisocyanate fractions are obtained.